2.7.1.136: macrolide 2'-kinase
This is an abbreviated version!
For detailed information about macrolide 2'-kinase, go to the full flat file.
Word Map on EC 2.7.1.136
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2.7.1.136
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erythromycin
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oleandomycin
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erythromycin-resistant
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phosphotransferases
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aminoglycoside
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self-transferable
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purine
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roxithromycin
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triphosphate
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itp
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repressor
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16-membered
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agarose
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2'-phosphate
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iodine
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edta
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macrolide-resistance
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aeruginosa
-
analysis
- 2.7.1.136
- erythromycin
- oleandomycin
-
erythromycin-resistant
-
phosphotransferases
- aminoglycoside
-
self-transferable
- purine
- roxithromycin
- triphosphate
- itp
- repressor
-
16-membered
- agarose
- 2'-phosphate
- iodine
- edta
-
macrolide-resistance
- aeruginosa
- analysis
Reaction
Synonyms
macrolide 2'-phosphotransferase, macrolide 2'-phosphotransferase II, macrolide 2'-phosphotransferase type I, macrolide 2'-phosphotransferase type II, Mph, MPH (2'), MPH(2'), MPH(2')-I, MPH(2')-II, mphA, mphB, phosphotransferase, macrolide 2'-
ECTree
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Crystallization
Crystallization on EC 2.7.1.136 - macrolide 2'-kinase
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purified isozyme MPH(2')-I in apoform and in complex with GTP analogues and six different macrolides (guanosine 5'-[beta,gamma-imido]triphosphate (GMPPNP) or guanosine diphosphate (GDP) and either a 14-membered lactone macrolide: erythromycin, oleandomycin, or clarithromycin, or the 15-membered lactone macrolide azithromycin), X-ray diffraction structure determination analysis at 1.2-1.6 A resolution, molecular replacement method, modeling. Despite the inclusion of MgCl2 in the crystallization experiments, no evidence of magnesium ions is observed in any of the MPH(2')-I electron density maps
purified isozyme MPH(2')-II in apoform and in complex with GTP analogues and six different macrolides (guanosine diphosphate (GDP) or GDP or GTPgS (guanosine 5'-O-[gamma-thio]triphosphate) and either a 14-membered lactone macrolide: erythromycin, oleandomycin, or clarithromycin, or the 15-membered lactone macrolide azithromycin), X-ray diffraction structure determination analysis at 1.31-1.65 A resolution, molecular replacement method, modeling. At least one divalent metal ion (either Mg2+ or Ca2+, based on the geometry and bond distances) from the crystallization solution is observed in the nucleotide binding pocket